Atypical parkinsonism combining α‐synuclein inclusions and polyglucosan body disease
Identifieur interne : 000417 ( France/Analysis ); précédent : 000416; suivant : 000418Atypical parkinsonism combining α‐synuclein inclusions and polyglucosan body disease
Auteurs : Elsa Krim [France] ; Anne Vital [France] ; Frederic Macia [France] ; Farid Yekhlef [France] ; François Tison [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2005-02.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Aged, Glial Fibrillary Acidic Protein (metabolism), Glucans (metabolism), Humans, Immunohistochemistry (methods), Inclusion Bodies (metabolism), Inclusion Bodies (pathology), Inclusion body, Lewy Bodies (metabolism), Lewy Bodies (pathology), Male, Multiple System Atrophy (etiology), Multiple System Atrophy (pathology), Nerve Tissue Proteins (metabolism), Nervous system diseases, Parkinsonian Disorders (complications), Parkinsonian Disorders (metabolism), Parkinsonian Disorders (pathology), Parkinsonism, Review Literature as Topic, Staining and Labeling (methods), Synucleins, adult polyglucosan body disease, alpha-Synuclein, multiple system atrophy, parkinsonism, α‐synuclein inclusions.
- MESH :
- chemical , metabolism : Glial Fibrillary Acidic Protein, Glucans, Nerve Tissue Proteins.
- complications : Parkinsonian Disorders.
- etiology : Multiple System Atrophy.
- metabolism : Inclusion Bodies, Lewy Bodies, Parkinsonian Disorders.
- methods : Immunohistochemistry, Staining and Labeling.
- pathology : Inclusion Bodies, Lewy Bodies, Multiple System Atrophy, Parkinsonian Disorders.
- Aged, Humans, Male, Review Literature as Topic, Synucleins, alpha-Synuclein.
Abstract
Adult polyglucosan body disease (APGBD) is a rare disorder affecting the central and peripheral nervous systems and in which parkinsonism is unusual. A 71‐year‐old man presented levodopa‐unresponsive parkinsonism with urinary incontinence and recurrent syncopes of 6 years standing masquerading as atypical parkinsonism of the multiple system atrophy (MSA‐P) type. Brain histopathology demonstrated massive accumulation of polyglucosan bodies particularly in the putamen. In addition, there were dense α‐synuclein–positive cytoplasmic oligodendroglial inclusions in the pons and in the middle cerebellar peduncle. These inclusions may be either due to the chance association of MSA‐P with APGBD, or pathologically related to APGBD. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20285
Affiliations:
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ISTEX:84501A6996AFFE9686105A527412308DBB3FDBB7Le document en format XML
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A 71‐year‐old man presented levodopa‐unresponsive parkinsonism with urinary incontinence and recurrent syncopes of 6 years standing masquerading as atypical parkinsonism of the multiple system atrophy (MSA‐P) type. Brain histopathology demonstrated massive accumulation of polyglucosan bodies particularly in the putamen. In addition, there were dense α‐synuclein–positive cytoplasmic oligodendroglial inclusions in the pons and in the middle cerebellar peduncle. These inclusions may be either due to the chance association of MSA‐P with APGBD, or pathologically related to APGBD. © 2004 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>France</li></country></list><tree><country name="France"><noRegion><name sortKey="Krim, Elsa" sort="Krim, Elsa" uniqKey="Krim E" first="Elsa" last="Krim">Elsa Krim</name></noRegion><name sortKey="Macia, Frederic" sort="Macia, Frederic" uniqKey="Macia F" first="Frederic" last="Macia">Frederic Macia</name><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name><name sortKey="Vital, Anne" sort="Vital, Anne" uniqKey="Vital A" first="Anne" last="Vital">Anne Vital</name><name sortKey="Yekhlef, Farid" sort="Yekhlef, Farid" uniqKey="Yekhlef F" first="Farid" last="Yekhlef">Farid Yekhlef</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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